NDC 68180-389 – Fenofibrate

Fenofibrate 145 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68180-389

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090856
Marketed since
August 1, 2020
Listing expires
December 31, 2026
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fenofibrate →

Package NDC codes (2)

Package NDCDescriptionSince
68180-389-02500 TABLET in 1 BOTTLE (68180-389-02)Aug 1, 2020
68180-389-0990 TABLET in 1 BOTTLE (68180-389-09)Aug 1, 2020

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